Tag | Content |
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EnhancerAtlas ID | HS048-20390 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:55386090-55386980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr2:55386657-55386672 | TGCTGACTCATTGAG | - | 6.26 | TCF3 | MA0522.2 | chr2:55386634-55386644 | AACACCTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_03190 | chr2:55386122-55386792 | Brain_Angular_Gyrus | SE_03921 | chr2:55385928-55386914 | Brain_Anterior_Caudate | SE_04845 | chr2:55385906-55398478 | Brain_Cingulate_Gyrus | SE_05873 | chr2:55385713-55398018 | Brain_Hippocampus_Middle | SE_06720 | chr2:55385708-55386989 | Brain_Hippocampus_Middle_150 | SE_07801 | chr2:55385879-55397743 | Brain_Inferior_Temporal_Lobe | SE_27564 | chr2:55386032-55386886 | Esophagus | SE_37014 | chr2:55381179-55387296 | HSMMtube | SE_43033 | chr2:55385985-55386944 | Lung | SE_49902 | chr2:55386057-55389484 | RPMI-8402 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I055150 | chr2 | 55377376 | 55387240 |
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Enhancer Sequence | CTGGGATTAC AGGCGTGAGC CACCGCACCC AGCCAAGCCC CACTCTTTTT TGCCAAAGTT 60 TCTTCTGGTA AAACATACCT ATAAAGAGAG ATTTATACTA AGGAGGCCCC CACCCAGCTC 120 AGCTGAAGGA AGAGAATGGG TGGGTGCTGA GGCTTCCTAT TTTGGGAAAT CAGTCAGTTC 180 TCTATGAGCA GAGCCTGGGC CTCTGGCCAA CAAGTCCTTG GAGAGAGGGA GAGCAACAAG 240 TCAGGGGCAG CTTTAGAGTA CTCCAGGGAG AGGGCAGCCT CAGCCCCGTG AGCACATGCT 300 AAAGTGACAC CACTATGACC TTGCCCCCTC CACTTCCACT GGGCAGGGAC CTGCTTCCCA 360 TGTGTGGCCC TGAGCCTACT GGGGAAGGGA TTGAGGGTGT ACTGCCCCTC CCCACAACAA 420 GGTCGGAGGG AGAACAGGCC CAGATCTGTC CTCTGCTCCA ATTTCCTCCT CAGAGAGGAA 480 GAGGTGGCTC CGCACAGCAG CTGTGTGACC CTTGGCAGTT TCTCATCTGT AAAAAAGTGA 540 CAGCAACACC TGCTTCATAG AATATGGTGC TGACTCATTG AGATGATGTC TGTGAAACAC 600 CTAACATGCA CTGGGTACTC AGCTAAGGGA GGGGGCATCC CTTCCTCCCA GCAGCAATTC 660 ATGAATTCTC AGGGAGCATC AGCCTCTCGT ACATCTTGTT CTGCACCATC AATGACAACC 720 TTCCCTAAAC CCCAAATATA GCTCTCTCTA TGCCAGCTGC ATATGCCTAT CTGCAGCTCC 780 TCCAGTTCCA TTCTGGCCAT TGGTTCTGCT GTATATTTTA TTATACAAAA TATATATTAT 840 ATACTTATAT AGTATTTCCC ACATACCCAG GACTCTTCTA AGACCTTTAT 890
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